CU20080165A7 - DERIVATIVES OF 1,2,4,5-TETRAHIDRO-3H-BENZAZEPINAS, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM - Google Patents
DERIVATIVES OF 1,2,4,5-TETRAHIDRO-3H-BENZAZEPINAS, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEMInfo
- Publication number
- CU20080165A7 CU20080165A7 CU20080165A CU20080165A CU20080165A7 CU 20080165 A7 CU20080165 A7 CU 20080165A7 CU 20080165 A CU20080165 A CU 20080165A CU 20080165 A CU20080165 A CU 20080165A CU 20080165 A7 CU20080165 A7 CU 20080165A7
- Authority
- CU
- Cuba
- Prior art keywords
- group
- optionally substituted
- hydrogen atom
- represent
- alkoxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D223/16—Benzazepines; Hydrogenated benzazepines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B55/00—Racemisation; Complete or partial inversion
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Abstract
Compuestos de fórmula (I): ESPACIO PARA FÓRMULA en la que: -R1 representa un átomo de hidrógeno o un grupo elegido entre cicloalquilo, bencilo y alquilo opcionalmente sustituido, -R2, R3, R4 y R5 representan cada uno un átomo de hidrógeno o un grupo hidroxi, metilo, -OSO2R10,- OCOR10, alcoxi opcionalmente sustituido, o bien R2 y R3, o R3 y R4, o R4 y R5 forman juntos un grupo -O-(CH2)q-O-, -O-CH=CH-O- o -O-CH=CH-, -R6, R7, R8 y R9 representan cada uno un átomo de hodrógeno o un grupo alcoxi, o bien R6 y R7, o R7 y R8, o R8 y R9 forman juntos un grupo -O-(CH2)q-O-, -R10 representa un grupo elegidoentre alcoxi C1-C6 lineal o ramificado, NR11R'11 y alquilo opcionalmente sustituido, -R11 y R'11 representan cada uno un átomo de hidrógeno o un grupo alquilo, o bien R11 y R'11 forman juntos, con el átomo de nitrógeno que les soporta, un heterociclo nitrogenado mono-o bicíclico opcionalmente sustituido, - X representa O, NH o CH2 - m yp representan cada uno 0 ó 1, - n y q representan cada uno 1 ó 2, en forma racémica o de isómeros ópticos, así como sus sales de adición con un ácido farmacéuticamente aceptable.Compounds of formula (I): SPACE FOR FORMULA in which: -R1 represents a hydrogen atom or a group chosen from cycloalkyl, benzyl and optionally substituted alkyl, -R2, R3, R4 and R5 each represent a hydrogen atom or a hydroxy, methyl group, -OSO2R10, - OCOR10, optionally substituted alkoxy, or R2 and R3, or R3 and R4, or R4 and R5 together form a group -O- (CH2) qO-, -O-CH = CH -O- or -O-CH = CH-, -R6, R7, R8 and R9 each represent a hydrogen atom or an alkoxy group, either R6 and R7, or R7 and R8, or R8 and R9 together form a group -O- (CH2) qO-, -R10 represents a group selected from linear or branched C1-C6 alkoxy, NR11R'11 and optionally substituted alkyl, -R11 and R'11 each represent a hydrogen atom or an alkyl group, or R11 and R'11 together form, with the nitrogen atom that supports them, an optionally substituted mono- or bicyclic nitrogen heterocycle, - X represents O, NH or CH2 - m and p each represents 0 or 1, - nyq represents They are each 1 or 2, in racemic form or optical isomers, as well as their addition salts with a pharmaceutically acceptable acid.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0706346A FR2920773B1 (en) | 2007-09-11 | 2007-09-11 | 1,2,4,5-TETRAHYDRO-3H-BENZAZEPINES DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CU20080165A7 true CU20080165A7 (en) | 2011-03-21 |
| CU23706B7 CU23706B7 (en) | 2011-10-05 |
Family
ID=39323822
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CU20080165A CU23706B7 (en) | 2007-09-11 | 2008-09-11 | DERIVATIVES OF 1,2,4,5-TETRAHIDRO-3H-BENZAZEPINAS, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
Country Status (45)
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2961105B1 (en) | 2010-06-15 | 2013-02-08 | Servier Lab | USE OF THE ASSOCIATION OF A SINUSAL IF CURRENT INHIBITOR AND AN INHIBITOR OF THE ANGIOTENSIN CONVERSION ENZYME FOR THE TREATMENT OF CARDIAC INSUFFICIENCY |
| EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| FR2984320B1 (en) * | 2011-12-20 | 2013-11-29 | Servier Lab | NOVEL PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID |
| FR2984319B1 (en) * | 2011-12-20 | 2013-12-27 | Servier Lab | NOVEL PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID |
| FR2988720B1 (en) * | 2012-03-27 | 2014-03-14 | Servier Lab | NOVEL PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID |
| TWI654180B (en) | 2012-06-29 | 2019-03-21 | 美商艾佛艾姆希公司 | Fungicidal heterocyclic carboxamide |
| FR3003859B1 (en) * | 2013-03-26 | 2015-03-13 | Servier Lab | "PROCESS FOR THE SYNTHESIS OF 7,8-DIMETHOXY-1,3-DIHYDRO-2H-3-BENZAZEPIN-2-ONE DERIVATIVES AND APPLICATION TO THE SYNTHESIS OF IVABRADINE" |
| US9333208B2 (en) | 2013-07-16 | 2016-05-10 | Movses H. Karakossian | HCN inhibitors affecting ganglion cell function and visual function |
| FR3020810B1 (en) * | 2014-05-06 | 2016-05-06 | Servier Lab | NEW SALT OF IVABRADINE AND PROCESS FOR PREPARING SAME |
| FR3046793B1 (en) * | 2016-01-14 | 2018-01-05 | Les Laboratoires Servier | NOVEL PHOSPHINAN DERIVATIVES AND AZAPHOSPHINANES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| US20230140818A1 (en) * | 2017-04-27 | 2023-05-04 | The University Of Hong Kong | Use of hcn inhibitors for treatment of cancer |
| CN112724001B (en) * | 2019-10-28 | 2022-12-13 | 鲁南制药集团股份有限公司 | Ivabradine chiral intermediate compound |
| CN113372274B (en) * | 2020-03-10 | 2023-03-24 | 鲁南制药集团股份有限公司 | Preparation method of ivabradine |
| CN113372273B (en) * | 2020-03-10 | 2023-05-09 | 鲁南制药集团股份有限公司 | Ivabradine intermediate compound IV |
| CN117715902A (en) * | 2021-08-31 | 2024-03-15 | 卫材R&D管理有限公司 | Process for producing monocyclic pyridine derivative |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3119874A1 (en) * | 1981-05-19 | 1982-12-09 | Dr. Karl Thomae Gmbh, 7950 Biberach | "BENZAZEPINE DERIVATIVES, THEIR PRODUCTION AND THEIR USE AS MEDICINAL PRODUCTS" |
| DE3418270A1 (en) | 1984-05-17 | 1985-11-21 | Dr. Karl Thomae Gmbh, 7950 Biberach | NEW AMINOTETRAL DERIVATIVES, MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF |
| GB8707120D0 (en) * | 1987-03-25 | 1987-04-29 | Pfizer Ltd | Antiarrhythmic agents |
| JPH02193971A (en) * | 1989-01-20 | 1990-07-31 | Yamanouchi Pharmaceut Co Ltd | Tri-substituted 2,3,4,5-tetrahydrobenzazepine derivative and intermediate thereof |
| FR2681862B1 (en) * | 1991-09-27 | 1993-11-12 | Adir Cie | NOVELS (BENZOCYCLOALKYL) ALKYLAMINES, THEIR PREPARATION PROCESS, AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| AU6971894A (en) * | 1993-05-27 | 1994-12-20 | Smithkline Beecham Laboratoires Pharmaceutiques | Anti-arrhythmic n-substituted 3-benzazepines or isoquinolines |
| TW527355B (en) * | 1997-07-02 | 2003-04-11 | Bristol Myers Squibb Co | Inhibitors of farnesyl protein transferase |
| US6514964B1 (en) * | 1999-09-27 | 2003-02-04 | Amgen Inc. | Fused cycloheptane and fused azacycloheptane compounds and their methods of use |
| FR2882554B1 (en) * | 2005-02-28 | 2007-05-04 | Servier Lab | IVABRADINE HYDROCHLORIDE BETA D-CRYSTALLINE FORM, PROCESS FOR PREPARING THE SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
| FR2894826B1 (en) | 2005-12-21 | 2010-10-22 | Servier Lab | NOVEL ASSOCIATION OF SINUSAL IF CURRENT INHIBITOR AND CALCIUM INHIBITOR AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
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2007
- 2007-09-11 FR FR0706346A patent/FR2920773B1/en not_active Expired - Fee Related
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2008
- 2008-08-19 PE PE2008001405A patent/PE20090620A1/en active IP Right Grant
- 2008-08-20 CR CR10229A patent/CR10229A/en unknown
- 2008-08-20 SG SG200806160-8A patent/SG151172A1/en unknown
- 2008-08-21 UY UY31305A patent/UY31305A1/en active IP Right Grant
- 2008-08-26 AP AP2008004589A patent/AP2384A/en active
- 2008-08-27 MY MYPI20083304A patent/MY143079A/en unknown
- 2008-08-28 AU AU2008207585A patent/AU2008207585B2/en not_active Ceased
- 2008-09-01 MX MX2008011164A patent/MX2008011164A/en active IP Right Grant
- 2008-09-02 TW TW097133661A patent/TWI374029B/en not_active IP Right Cessation
- 2008-09-02 CA CA2639349A patent/CA2639349C/en active Active
- 2008-09-03 ZA ZA2008/07586A patent/ZA200807586B/en unknown
- 2008-09-04 UA UAA200810902A patent/UA100003C2/en unknown
- 2008-09-05 JP JP2008227956A patent/JP4932805B2/en not_active Expired - Fee Related
- 2008-09-08 MA MA31219A patent/MA30315B1/en unknown
- 2008-09-08 HN HN2008001393A patent/HN2008001393A/en unknown
- 2008-09-08 CL CL2008002654A patent/CL2008002654A1/en unknown
- 2008-09-09 AR ARP080103906A patent/AR068386A1/en active IP Right Grant
- 2008-09-09 US US12/283,110 patent/US8076325B2/en not_active Expired - Fee Related
- 2008-09-09 PA PA20088795301A patent/PA8795301A1/en unknown
- 2008-09-10 EA EA200801828A patent/EA014756B1/en unknown
- 2008-09-10 JO JO2008404A patent/JO2652B1/en active
- 2008-09-10 KR KR1020080089213A patent/KR101078076B1/en active IP Right Grant
- 2008-09-10 SA SA08290567A patent/SA08290567B1/en unknown
- 2008-09-10 NZ NZ571143A patent/NZ571143A/en not_active IP Right Cessation
- 2008-09-10 EC EC2008008731A patent/ECSP088731A/en unknown
- 2008-09-10 NI NI200800247A patent/NI200800247A/en unknown
- 2008-09-11 DK DK08290851.8T patent/DK2036892T3/en active
- 2008-09-11 WO PCT/FR2008/001268 patent/WO2009066041A2/en active Application Filing
- 2008-09-11 ME MEP-2010-45A patent/ME00981B/en unknown
- 2008-09-11 CU CU20080165A patent/CU23706B7/en active IP Right Grant
- 2008-09-11 DE DE602008000786T patent/DE602008000786D1/en active Active
- 2008-09-11 PL PL08290851T patent/PL2036892T3/en unknown
- 2008-09-11 SI SI200830030T patent/SI2036892T1/en unknown
- 2008-09-11 PT PT08290851T patent/PT2036892E/en unknown
- 2008-09-11 BR BRPI0804091A patent/BRPI0804091B8/en not_active IP Right Cessation
- 2008-09-11 CN CN2008102135506A patent/CN101386594B/en not_active Expired - Fee Related
- 2008-09-11 AT AT08290851T patent/ATE460401T1/en active
- 2008-09-11 CO CO08095781A patent/CO6020016A1/en active IP Right Grant
- 2008-09-11 EP EP08290851A patent/EP2036892B1/en active Active
- 2008-09-11 ES ES08290851T patent/ES2342511T3/en active Active
- 2008-09-11 RS RSP-2010/0245A patent/RS51305B/en unknown
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2009
- 2009-08-24 HK HK09107750.6A patent/HK1129667A1/xx not_active IP Right Cessation
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2010
- 2010-05-11 HR HR20100259T patent/HRP20100259T1/en unknown
- 2010-05-17 CY CY20101100438T patent/CY1110034T1/en unknown
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